Canonical Allele Identifier: CA2429869100
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534521T= , CM000685.2:g.53534521T= GRCh38
NC_000023.10:g.53561482T= , CM000685.1:g.53561482T= GRCh37
NC_000023.9:g.53578207T= NCBI36
NG_016261.2:g.157213A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12610A= ENSP00000515693.1:p.Ile4204=
ENST00000262854.11:c.12826A= MANE Select ENSP00000262854.6:p.Ile4276=
ENST00000262854.10:c.12826A= ENSP00000262854.6:p.Ile4276=
ENST00000342160.7:c.12826A= ENSP00000340648.3:p.Ile4276=
ENST00000426907.5:c.3293A=
ENST00000488459.1:n.139A=
ENST00000612484.4:c.12799A= ENSP00000479451.1:p.Ile4267=
NM_031407.6:c.12826A= NP_113584.3:p.Ile4276=
XM_005261965.2:c.12826A= XP_005262022.1:p.Ile4276=
XM_011530746.1:c.13075A= XP_011529048.1:p.Ile4359=
XM_011530747.1:c.13075A= XP_011529049.1:p.Ile4359=
XM_011530748.1:c.13075A= XP_011529050.1:p.Ile4359=
XM_011530749.1:c.13075A= XP_011529051.1:p.Ile4359=
XM_011530750.1:c.13075A= XP_011529052.1:p.Ile4359=
XM_011530751.1:c.13075A= XP_011529053.1:p.Ile4359=
XM_011530752.1:c.13072A= XP_011529054.1:p.Ile4358=
XM_011530753.1:c.13030A= XP_011529055.1:p.Ile4344=
XM_011530754.1:c.13027A= XP_011529056.1:p.Ile4343=
XM_011530755.1:c.13024A= XP_011529057.1:p.Ile4342=
XM_011530756.1:c.12976A= XP_011529058.1:p.Ile4326=
XM_011530757.1:c.12673A= XP_011529059.1:p.Ile4225=
XM_005261965.4:c.12826A= XP_005262022.1:p.Ile4276=
XM_011530751.2:c.13075A= XP_011529053.1:p.Ile4359=
XM_017029191.1:c.13207A= XP_016884680.1:p.Ile4403=
XM_017029192.1:c.13204A= XP_016884681.1:p.Ile4402=
XM_017029193.1:c.13186A= XP_016884682.1:p.Ile4396=
XM_017029194.1:c.13162A= XP_016884683.1:p.Ile4388=
XM_017029195.1:c.13159A= XP_016884684.1:p.Ile4387=
XM_017029196.1:c.13156A= XP_016884685.1:p.Ile4386=
XM_017029197.1:c.13108A= XP_016884686.1:p.Ile4370=
XM_017029198.2:c.13096A= XP_016884687.1:p.Ile4366=
XM_017029199.1:c.13096A= XP_016884688.1:p.Ile4366=
XM_017029200.1:c.13096A= XP_016884689.1:p.Ile4366=
XM_017029201.1:c.13096A= XP_016884690.1:p.Ile4366=
XM_017029202.1:c.13096A= XP_016884691.1:p.Ile4366=
XM_017029203.1:c.13096A= XP_016884692.1:p.Ile4366=
XM_017029204.1:c.12958A= XP_016884693.1:p.Ile4320=
XM_017029206.1:c.12805A= XP_016884695.1:p.Ile4269=
XM_024452322.1:c.13075A= XP_024308090.1:p.Ile4359=
NM_031407.7:c.12826A= MANE Select NP_113584.3:p.Ile4276=